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首页> 外文期刊>Journal of Pharmacy and Pharmaceutical Sciences >Assessing the Physicochemical Stability of a Compounded Neonatal Trace Element Solution
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Assessing the Physicochemical Stability of a Compounded Neonatal Trace Element Solution

机译:评估复合新生儿微量元素溶液的理化稳定性

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PURPOSE: Alberta Health Services (AHS) recommends the adoption of a new neonatal multi-trace element formulation containing zinc sulfate, copper sulfate, selenious acid and sodium iodide to be compounded internally in appropriate AHS pharmacies. The objective of this study was to assess the physicochemical stability of this formulation under commonly used storage conditions. METHOD: Three batches of trace element solution were compounded by University of Alberta Hospital pharmacy staff using sterile compounding procedures. Appropriate amount of zinc sulfate (500 mg/mL), copper sulfate (40 mg/mL), selenious acid (4 mg/mL), sodium iodide (2 mg/mL) and sterile water for injection were mixed. Samples from each batch were divided in individual vials and syringes for each time point and kept protected from light either at room temperature (15–30°C) or fridge (2-8°C). Vial samples were also kept at room temperature for 12 h and then transferred to fridge. Vial samples were analyzed at time 0, 12 h, and 1, 3, 7, 9, 30, 60, 90 days for their physical appearance and pH, then centrifuged and assessed for the soluble zinc (atomic absorption), copper (atomic absorption), selenium (ICP-MS) and iodine (HPLC and ICP-MS) concentrations. Syringe samples were tested at time 0 and 12 h for element concentrations. RESULTS: Under all storage conditions, when stored in vials, samples’ appearance, pH and soluble zinc, copper and selenium concentrations stayed within the USP acceptable limits up to 90 days. Iodine concentration was within the permitted limits only up to 7 days. The USP recommended HPLC method of iodine analysis seemed inadequate for this preparation and needed modifications, through frequent washing of the column with KI (2 %) solution. Samples kept in syringes at room temperature, showed lower than permitted concentration of Zn at 12h in this study. CONCLUSION: The AHS neonatal multi-trace element formulation seem to be physio-chemically stable up to 7 days in all three storage conditions when kept in vials. A decline in iodine concentration is seen after 7 days irrespective of storage conditions.?This article is open to POST-PUBLICATION REVIEW. Registered readers (see “For Readers”) may comment by clicking on ABSTRACT on the issue’s contents page.
机译:目的:艾伯塔省卫生服务(AHS)建议采用一种新的新生儿多微量元素配方,其中应在适当的AHS药房内部配制包含硫酸锌,硫酸铜,亚硒酸和碘化钠的化合物。这项研究的目的是评估该制剂在常用储存条件下的物理化学稳定性。方法:由阿尔伯塔大学医院药房的工作人员按照无菌配制方法配制了三批微量元素溶液。混合适量的硫酸锌(500 mg / mL),硫酸铜(40 mg / mL),亚硒酸(4 mg / mL),碘化钠(2 mg / mL)和无菌注射用水。将每个批次的样品在每个时间点分成单独的小瓶和注射器,并在室温(15–30°C)或冰箱(2-8°C)下避光保存。小瓶样品也要在室温下放置12小时,然后转移到冰箱中。在时间0、12小时和1、3、7、9、30、60、90天时分析样品瓶的物理外观和pH值,然后离心并评估可溶性锌(原子吸收),铜(原子吸收) ),硒(ICP-MS)和碘(HPLC和ICP-MS)浓度。在时间0和12小时测试了注射器样品的元素浓度。结果:在所有储存条件下,当储存在小瓶中时,样品的外观,pH值以及可溶性锌,铜和硒的浓度在90天之内都保持在USP可接受的范围内。碘浓度最多只能达到7天。 USP建议的碘分析HPLC方法似乎不足以进行此制备,需要进行修饰,方法是经常用KI(2%)溶液洗涤色谱柱。在这项研究中,室温下保存在注射器中的样品显示低于允许的Zn浓度。结论:当放在小瓶中时,在所有三种存储条件下,AHS新生儿多痕量元素配方在理化稳定性上似乎长达7天。无论储存条件如何,在7天后碘浓度都会下降。本文接受后发表审查。已注册的读者(请参阅“针对读者”)可以通过在问题目录页面上单击摘要来发表评论。

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